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Synthesis of 1S,5R- and 1R,5S-glycoluriles by diastereospecific α-ureidoalkylation of (S)/(R)-N-carbamoyl-α-amino acids with 4,5-dihydroxyimidazolidin-2-one
A diastereospecific method for the synthesis of individual enantiomers of 1 S ,5 R - and 1 R ,5 S -glycoluriles has been developed based on the α-ureidoalkylation of ( S )/( R )- N -carbamoyl-α-amino acids with 4,5-dihydroxyimidazolidin-2-one.
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Published in: | Mendeleev communications 2004, Vol.14 (6), p.253-255 |
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Main Authors: | , , , , , , |
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Language: | English |
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container_end_page | 255 |
container_issue | 6 |
container_start_page | 253 |
container_title | Mendeleev communications |
container_volume | 14 |
creator | Chikunov, Il'ya E Kravchenko, Angelina N Belyakov, Pavel A Lyssenko, Konstantin A Baranov, Vladimir V Lebedev, Oleg V Makhova, Nina N |
description | A diastereospecific method for the synthesis of individual enantiomers of 1
S
,5
R
- and 1
R
,5
S
-glycoluriles has been developed based on the α-ureidoalkylation of (
S
)/(
R
)-
N
-carbamoyl-α-amino acids with 4,5-dihydroxyimidazolidin-2-one. |
doi_str_mv | 10.1070/MC2004v014n06ABEH002050 |
format | article |
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S
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R
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S
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R
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issn | 0959-9436 1364-557X |
language | eng |
recordid | cdi_crossref_primary_10_1070_MC2004v014n06ABEH002050 |
source | ScienceDirect Journals |
title | Synthesis of 1S,5R- and 1R,5S-glycoluriles by diastereospecific α-ureidoalkylation of (S)/(R)-N-carbamoyl-α-amino acids with 4,5-dihydroxyimidazolidin-2-one |
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